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Structure of 908338-42-1
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This trifluoromethylated sulfonamide integrates a sterically encumbered dioxaphosphepine scaffold, delivering enhanced stability and selective reactivity in transition metal-catalyzed transformations. The electron-deficient trifluoromethyl group modulates electronic properties, while the oxido-diphenyl substitution pattern supports robust chiral induction in asymmetric synthesis workflows under standard conditions.
1,1,1-Trifluoro-N-[(11bS)-4-oxido-2,6-diphenyldinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-yl]methanesulfonamide serves as a stable, bench-ready phosphine oxide reagent enabling stereoselective transformations in complex molecule synthesis. Its rigid heterocyclic framework and trifluoromethyl sulfonamide group provide excellent functional group tolerance and ease of purification. This compound functions as a key building block in catalytic asymmetric synthesis, particularly for constructing sterically congested scaffolds under mild conditions.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P280-P302+P352
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Lot numbers can be found on the outside label of a product: